.Organisation/Company: Institut d'Investigacio Biomedica de Bellvitge (IDIBELL)Department: RRHHResearch Field: Biological sciences » BiologyResearcher Profile: First Stage Researcher (R1) PositionsCountry: SpainApplication Deadline: 16 Dec 2024 - 23:59 (Europe/Madrid)Type of Contract: PermanentJob Status: Full-timeOffer Starting Date: 4 Dec 2024Is the job funded through the EU Research Framework Programme? Not funded by a EU programmeIs the Job related to staff position within a Research Infrastructure? NoOffer DescriptionAbout the research groupICO- L'Hospitalet is a reference hospital for clinical research in cancer. Their two units (UIC and UFF1) have been participating in 612 clinical trials with active recruitment or current activities during 2023 and 663 patients decided to participate in them. Many of these trials are testing the most promising therapies in cancer, and investigators involved in them are specialized and up-to-date with the latest advances in new treatments. UIC and UFF1 units have the best professionals who carry out the most demanding clinical trials.About the roleSupervision and distribution of tasks and charges of the different study coordinators, data entries, and regulatory personnel (allocation and follow-up).Supervision that personnel executes standard operating procedures according to the quality plan (daily operations, non-conformities, support for trials audits and inspections).Personnel management (permissions and holidays, work from home, and location managements and sick leave support).Personnel meetings with principal investigators and writing minutes.Coordinated work with other areas of UIC (economic management, etc).Job requirementsProfessional experienceAt minimum 2 years as study coordinator.Experience with clinical trials audits or inspections as study coordinator.Education and trainingEducation in clinical trials and clinical research.Education in Good Clinical Practices.Technical & soft skillsOffice (Outlook, Excel, Word), internet, patients files.Personnel management and leadership of labor relations. To organize, order, and perform different activities with knowledge of their influence on the final outcome of a process. Understand the points of view of other people, give help. Ability to work under pressure.LanguagesGood command of the English language.We will value, but not required:Experience as Clinical trials Monitor.Familiarity with SAP Argos Electronic Medical Record system.Previous experience in data management of oncology studies.Previous experience in clinical trials (other than cancer).Application:All applications must include the following:A motivation letter addressed to Valentin Navarro Perez.A CV including contact information.Contact details of two referees.Selection processPre-selection: The pre-selection process will consist of an eligibility check based on qualifications and expertise reflected in the candidate's CV